Abstract Slide 1 MetaboLogic
Biochemistry
Quiz 2025
22.07. 2025
Department of Biochemistry, KIMS
Warmly welcomes all
Abstract Slide 2
Prof. Dr
Viyatprajna
Acharya
Prof Dr Jyotirmayee
Bahinipati
The Quiz Masters
The Scorers
Dr Subhashree
Nath
Dr. Ananya
Samantaray
General Round-I
1. N-acetylneuraminic acid
(NANA) is present in
a) Phospholipid
b) Cerebroside
c) Ganglioside
d) TG
2. The main lipid present in plasma
membrane is
a. Cholesterol
b. Triglyceride
c. Phospholipid
d. Fatty acids
3. The smallest monosaccharide having stable furanose
ring str is
a) Erythrose
b) Ribose
c) Glucose
d) Fructose
4. DNA absorbs light at wavelength of
a) 260nm
b) 360nm
c) 460nm
d) 560nm
5. Which of the following is the most electronegative constituent of
ETC?
a) O2
b) NADH dehydrogenase
c) CoQ
d) Cytochrome oxidase
6. What is the ratio of ECF/ICF volume in humans?
a) 1:2
b) 2:1
c) 1:3
d) 3:1
General Round-II
1. Identify the structure
2. Identify the structure
3. Identify the molecule represented by the following structure
4. Identify the molecule shown in the diagram.
5. Identify the structure and mention its use
6. Identify the structure and mention its use
Abstract Slide 5
SCORE??
Clinical Case Scenario
1. Baby R, a 7-day-old full-term female infant, presents with
vomiting, poor feeding, lethargy, jaundice, and hepatomegaly.
Urine is positive for reducing substances but negative for glucose.
Blood glucose is low. Blood glucose -50mg%, Uric acid- 10 mg%,
Lactic acid- 15mmol/L, Plasma cholesterol- 300mg% and .
What is the most likely diagnosis?
A. Neonatal jaundice
B. Classic galactosemia
C. Crigler–Najjar syndrome
D. Hereditary fructose intolerance
2. A 3-day-old male infant is brought to the emergency with vomiting,
lethargy, and rapid breathing. Blood tests reveal:
Plasma ammonia: Very high, Blood pH: 7.48, Serum glucose: Normal
No ketone bodies in urine, No acidosis
There is no history of infection or birth trauma. Urine organic acid levels
are normal.
What is the most likely diagnosis?
A. Maple syrup urine disease
B. Diabetic ketoacidosis
C. Ornithine Transcarbamoylase deficiency
D. Galactosemia
3. A 55-year-old vegetarian man presents with complaints of fatigue, tingling
sensation in his feet, and difficulty in walking. On examination, he has pallor, a
beefy red tongue, and diminished position sense in the lower limbs. Blood tests
show: Hemoglobin: 8.5 g/dL, MCV: 110 fL (macrocytic), Serum B12: 150pg/ml,
Peripheral smear: Hypersegmented neutrophils.
Which of the following metabolic reactions is most likely impaired in this
patient?
A. Conversion of methylmalonyl-CoA to succinyl-CoA
B. Conversion of pyruvate to acetyl-CoA
C. Transamination of alanine to pyruvate
D. Conversion of succinyl-CoA to heme
4. A 3-year-old boy is brought to the pediatrician due to delayed milestones, aggressive
behavior, and self-mutilation (biting his lips and fingers). His parents report that he
also has orange sandy crystals in the diaper. Lab tests show:
Serum uric acid: 10mg/dl, Neurological signs: Spasticity and dystonia
Which of the following enzyme deficiencies is most likely responsible for his
condition?
A. Adenosine deaminase
B. Hypoxanthine-guanine phosphoribosyltransferase (HGPRT)
C. Galactose-1-P uridyl transferase
D. Glucose-6-phosphatase
5.A 16-year-old girl presents with hyperextensible skin,
hypermobile joints, and a history of frequent bruising. She also
reports delayed wound healing. Her maternal uncle had died suddenly
of a ruptured aortic aneurysm.
Which of the following biochemical defects is most likely involved
in her condition?
A. Defective hydroxylation of proline and lysine residues in
collagen
B. Deficient glycosylation of collagen
C. Defective cross-linking of collagen fibrils due to lysyl oxidase
deficiency
D. Mutations in collagen genes affecting triple helix structure
6. A 32-year-old woman presents for a routine health check-up. She
has no specific symptoms. Her thyroid profile shows the following:
TSH: 7.2 mIU/L (Normal: 0.4–4.0)Free T4: NormalAnti-TPO antibodies:
Positive. Her FBS was found lower than PPBS.
What is the most appropriate interpretation of her thyroid function
tests?
A. Overt hypothyroidism
B. Subclinical hypothyroidism
C. Euthyroid sick syndrome
D. Central hypothyroidism
Abstract Slide 5
SCORE??
Pictorial Round
1. What is the primary component of
the structure shown:
a) Proteins
b) Carbohydrates
c) Phospholipids
d) Nucleic acids
2. Identify the condition.
3. Identify the plot and mention its significance.
4. Identify the crystals.
5. Identify the ophthalmic condition.
6. Identify the type of enzyme inhibition.
Abstract Slide 3
SCORE??
Instrumentation round
Q1. Identify the Instrument
Q2. Identify the Instrument
?
Q3. Identify the Instrument
Q 4. Mention the technique used
Q5. Identify the Tube and mention
its use
Q6. Sharps like needles and broken glass would go
to which Bin?
Abstract Slide 5
SCORE??
Step Ladder Round
I am an enzymatic cardiac marker raised after 24 hours of
heart attack and can be found in blood after 8-10 days
I am also found in RBC, brain, liver, skeletal muscle
I am a tetramer
I have 4 other siblings
1
I’m a water-soluble vitamin, in high sustained
release dose I can lead to hepatotoxicity
I am a bridge between carbohydrates and ATP, aiding
dehydrogenases in their harvest.
I’m synthesized from an aromatic amino acid.
My deficiency scars the skin and mind, especially
when sunlight strikes.
2
I’m an amino acid, with a net positive charge at
physiological pH and my presence boosts wound
healing and immune responses.
I become essential for infants and in trauma
and illness
I contribute to a cyclic process crucial for nitrogen
balance.
I contain a guanidine group
3
I’m a hidden flaw, an enzymopathy, often unnoticed until
challenged by nature or medicine.
Infection, beans, or a bitter pill for malaria may expose
me.
My victims suffer oxidative stress but can’t regenerate a
reducing agent.
I leave behind Heinz bodies and bite cells on a smear.
4
I’m an organelle known as microbody
My marker enzyme is catalase
I’m involved in very long chain fatty
acid metabolism
I remove unwanted peroxides and free
radicals from the cell
5
I’m a reducing equivalent helping
Oxidoreductases and a part of 2nd
complex of
ETC
I have an isoalloxazine ring
I’m a derivative of Warburg’s yellow enzyme
I can produce 2 ATP in ETC
6
Abstract Slide 3
SCORE??
Rapid fire round
1
1) Name an ectoenzyme
2) Reference range of cholesterol
3) Alpha1 antitrypsin is an acute phase protein T/F
4) Primary structure of protein contains sulfide
bridges- T/F
5) Cyanide inhibits which complex of ETC?
6) What is the DNA repair defect in Xeroderma
pigmentosa?
2
1) Reference range of AST?
2) Bile salts appear in urine in hemolytic jaundice- T/F
3) Which fraction of HDL-C is bad cholesterol?
4) How much is SDA of protein?
5) Lac Y codes for which enzyme?
6) Iodine number measures--
3
1) UGA codes for which amino acid?
2) Collagen triple helix has secondary protein structure- T/F?
3) Phrynoderma is a condition seen due to deficiency of?
4) Reference range of serum calcium?
5) Schilling test is done to find out—
6) Most effective blood buffer is--
4
1) RDA of thiamine (Vitamin B1)?
2) pH of urine is acidic in respiratory acidosis- T/F?
3) Leukotrienes are synthesised by which pathway?
4) What is translocation in translation process?
5) Statin group of drugs inhibit which enzyme?
6) First purine to be produced is--
Abstract Slide 4
FINAL SCORE???
Instructional Slide Identify the chart
•A child presents with failure to thrive, steatorrhea, and ataxia.
Peripheral smear shows acanthocytes. Serum LDL and chylomicrons
are undetectable. Identify the disorder and explain the lipid
abnormality.
•Which is the most common epigenetic mechanism?
Thank you !!!
MetaboLogic
Biochemistry Quiz 2025
This is to certify that Mr/Ms------------------------------------------------------participated and won
--------------------------------------position in “MetaboLogic”, Biochemistry Quiz competition
conducted on Dt. 28.06.2025 at KIMS, Bhubaneswar.
Organizing Chairman
Prof. Tapaswini Pradhan
HOD Biochemistry
Organizing Secretary
Prof. Viyatprajna Acharya
Principal
AVM Prof. R.C. Das

Biochemistry Quiz 2025-Metabologic PowerPoint

  • 1.
    Abstract Slide 1MetaboLogic Biochemistry Quiz 2025 22.07. 2025 Department of Biochemistry, KIMS Warmly welcomes all
  • 3.
    Abstract Slide 2 Prof.Dr Viyatprajna Acharya Prof Dr Jyotirmayee Bahinipati The Quiz Masters
  • 4.
  • 5.
  • 6.
    1. N-acetylneuraminic acid (NANA)is present in a) Phospholipid b) Cerebroside c) Ganglioside d) TG
  • 7.
    2. The mainlipid present in plasma membrane is a. Cholesterol b. Triglyceride c. Phospholipid d. Fatty acids
  • 8.
    3. The smallestmonosaccharide having stable furanose ring str is a) Erythrose b) Ribose c) Glucose d) Fructose
  • 9.
    4. DNA absorbslight at wavelength of a) 260nm b) 360nm c) 460nm d) 560nm
  • 10.
    5. Which ofthe following is the most electronegative constituent of ETC? a) O2 b) NADH dehydrogenase c) CoQ d) Cytochrome oxidase
  • 11.
    6. What isthe ratio of ECF/ICF volume in humans? a) 1:2 b) 2:1 c) 1:3 d) 3:1
  • 12.
  • 13.
    1. Identify thestructure
  • 14.
    2. Identify thestructure
  • 15.
    3. Identify themolecule represented by the following structure
  • 16.
    4. Identify themolecule shown in the diagram.
  • 17.
    5. Identify thestructure and mention its use
  • 18.
    6. Identify thestructure and mention its use
  • 19.
  • 20.
  • 21.
    1. Baby R,a 7-day-old full-term female infant, presents with vomiting, poor feeding, lethargy, jaundice, and hepatomegaly. Urine is positive for reducing substances but negative for glucose. Blood glucose is low. Blood glucose -50mg%, Uric acid- 10 mg%, Lactic acid- 15mmol/L, Plasma cholesterol- 300mg% and . What is the most likely diagnosis? A. Neonatal jaundice B. Classic galactosemia C. Crigler–Najjar syndrome D. Hereditary fructose intolerance
  • 22.
    2. A 3-day-oldmale infant is brought to the emergency with vomiting, lethargy, and rapid breathing. Blood tests reveal: Plasma ammonia: Very high, Blood pH: 7.48, Serum glucose: Normal No ketone bodies in urine, No acidosis There is no history of infection or birth trauma. Urine organic acid levels are normal. What is the most likely diagnosis? A. Maple syrup urine disease B. Diabetic ketoacidosis C. Ornithine Transcarbamoylase deficiency D. Galactosemia
  • 23.
    3. A 55-year-oldvegetarian man presents with complaints of fatigue, tingling sensation in his feet, and difficulty in walking. On examination, he has pallor, a beefy red tongue, and diminished position sense in the lower limbs. Blood tests show: Hemoglobin: 8.5 g/dL, MCV: 110 fL (macrocytic), Serum B12: 150pg/ml, Peripheral smear: Hypersegmented neutrophils. Which of the following metabolic reactions is most likely impaired in this patient? A. Conversion of methylmalonyl-CoA to succinyl-CoA B. Conversion of pyruvate to acetyl-CoA C. Transamination of alanine to pyruvate D. Conversion of succinyl-CoA to heme
  • 24.
    4. A 3-year-oldboy is brought to the pediatrician due to delayed milestones, aggressive behavior, and self-mutilation (biting his lips and fingers). His parents report that he also has orange sandy crystals in the diaper. Lab tests show: Serum uric acid: 10mg/dl, Neurological signs: Spasticity and dystonia Which of the following enzyme deficiencies is most likely responsible for his condition? A. Adenosine deaminase B. Hypoxanthine-guanine phosphoribosyltransferase (HGPRT) C. Galactose-1-P uridyl transferase D. Glucose-6-phosphatase
  • 25.
    5.A 16-year-old girlpresents with hyperextensible skin, hypermobile joints, and a history of frequent bruising. She also reports delayed wound healing. Her maternal uncle had died suddenly of a ruptured aortic aneurysm. Which of the following biochemical defects is most likely involved in her condition? A. Defective hydroxylation of proline and lysine residues in collagen B. Deficient glycosylation of collagen C. Defective cross-linking of collagen fibrils due to lysyl oxidase deficiency D. Mutations in collagen genes affecting triple helix structure
  • 26.
    6. A 32-year-oldwoman presents for a routine health check-up. She has no specific symptoms. Her thyroid profile shows the following: TSH: 7.2 mIU/L (Normal: 0.4–4.0)Free T4: NormalAnti-TPO antibodies: Positive. Her FBS was found lower than PPBS. What is the most appropriate interpretation of her thyroid function tests? A. Overt hypothyroidism B. Subclinical hypothyroidism C. Euthyroid sick syndrome D. Central hypothyroidism
  • 27.
  • 28.
  • 29.
    1. What isthe primary component of the structure shown: a) Proteins b) Carbohydrates c) Phospholipids d) Nucleic acids
  • 30.
    2. Identify thecondition.
  • 31.
    3. Identify theplot and mention its significance.
  • 32.
    4. Identify thecrystals.
  • 33.
    5. Identify theophthalmic condition.
  • 34.
    6. Identify thetype of enzyme inhibition.
  • 35.
  • 36.
  • 37.
    Q1. Identify theInstrument
  • 38.
    Q2. Identify theInstrument ?
  • 39.
    Q3. Identify theInstrument
  • 40.
    Q 4. Mentionthe technique used
  • 41.
    Q5. Identify theTube and mention its use
  • 42.
    Q6. Sharps likeneedles and broken glass would go to which Bin?
  • 43.
  • 44.
  • 45.
    I am anenzymatic cardiac marker raised after 24 hours of heart attack and can be found in blood after 8-10 days I am also found in RBC, brain, liver, skeletal muscle I am a tetramer I have 4 other siblings 1
  • 46.
    I’m a water-solublevitamin, in high sustained release dose I can lead to hepatotoxicity I am a bridge between carbohydrates and ATP, aiding dehydrogenases in their harvest. I’m synthesized from an aromatic amino acid. My deficiency scars the skin and mind, especially when sunlight strikes. 2
  • 47.
    I’m an aminoacid, with a net positive charge at physiological pH and my presence boosts wound healing and immune responses. I become essential for infants and in trauma and illness I contribute to a cyclic process crucial for nitrogen balance. I contain a guanidine group 3
  • 48.
    I’m a hiddenflaw, an enzymopathy, often unnoticed until challenged by nature or medicine. Infection, beans, or a bitter pill for malaria may expose me. My victims suffer oxidative stress but can’t regenerate a reducing agent. I leave behind Heinz bodies and bite cells on a smear. 4
  • 49.
    I’m an organelleknown as microbody My marker enzyme is catalase I’m involved in very long chain fatty acid metabolism I remove unwanted peroxides and free radicals from the cell 5
  • 50.
    I’m a reducingequivalent helping Oxidoreductases and a part of 2nd complex of ETC I have an isoalloxazine ring I’m a derivative of Warburg’s yellow enzyme I can produce 2 ATP in ETC 6
  • 51.
  • 52.
  • 53.
    1 1) Name anectoenzyme 2) Reference range of cholesterol 3) Alpha1 antitrypsin is an acute phase protein T/F 4) Primary structure of protein contains sulfide bridges- T/F 5) Cyanide inhibits which complex of ETC? 6) What is the DNA repair defect in Xeroderma pigmentosa?
  • 54.
    2 1) Reference rangeof AST? 2) Bile salts appear in urine in hemolytic jaundice- T/F 3) Which fraction of HDL-C is bad cholesterol? 4) How much is SDA of protein? 5) Lac Y codes for which enzyme? 6) Iodine number measures--
  • 55.
    3 1) UGA codesfor which amino acid? 2) Collagen triple helix has secondary protein structure- T/F? 3) Phrynoderma is a condition seen due to deficiency of? 4) Reference range of serum calcium? 5) Schilling test is done to find out— 6) Most effective blood buffer is--
  • 56.
    4 1) RDA ofthiamine (Vitamin B1)? 2) pH of urine is acidic in respiratory acidosis- T/F? 3) Leukotrienes are synthesised by which pathway? 4) What is translocation in translation process? 5) Statin group of drugs inhibit which enzyme? 6) First purine to be produced is--
  • 57.
  • 58.
  • 59.
    •A child presentswith failure to thrive, steatorrhea, and ataxia. Peripheral smear shows acanthocytes. Serum LDL and chylomicrons are undetectable. Identify the disorder and explain the lipid abnormality. •Which is the most common epigenetic mechanism? Thank you !!!
  • 60.
    MetaboLogic Biochemistry Quiz 2025 Thisis to certify that Mr/Ms------------------------------------------------------participated and won --------------------------------------position in “MetaboLogic”, Biochemistry Quiz competition conducted on Dt. 28.06.2025 at KIMS, Bhubaneswar. Organizing Chairman Prof. Tapaswini Pradhan HOD Biochemistry Organizing Secretary Prof. Viyatprajna Acharya Principal AVM Prof. R.C. Das